A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1123185



Internal ID18910991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:63145351..63145401hg38UCSC Ensembl
Outerchr18:60812584..60812634hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3972179
SamplesKWS2
Known GenesBCL2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1123185
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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